Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 10, 2023. (Total: 223917Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 16 (of 16 Records)

Query Trace: Vasculitis and MEFV[original query]
Mutations in the gene for familial Mediterranean fever: do they predispose to inflammation?
The Journal of rheumatology 2003 Sep 30 (9): 2014-8.
Ozen Seza, Bakkaloglu Aysin, Yilmaz Engin, Duzova Ali, Balci Banu, Topaloglu Rezan, Besbas Nesr
E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever.
Annals of the rheumatic diseases 2005 May 64 (5): 750-2.
Topaloglu R, Ozaltin F, Yilmaz E, Ozen S, Balci B, Besbas N, Bakkaloglu
Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis.
Scandinavian journal of rheumatology 0 36 (1): 48-52.
Rabinovich E, Shinar Y, Leiba M, Ehrenfeld M, Langevitz P, Livneh
Lack of association between E148Q MEFV variant and Kawasaki disease.
Human immunology 2009 Jun 70 (6): 468-71.
Yamaguchi Kenichiro, Ikeda Kazuyuki, Ihara Kenji, Takada Hidetoshi, Kusuhara Koichi, Hara Toshi
MEFV gene mutations (M694V, V726A, M680I, and A744S) in Iranian children with Henoch-Schönlein purpura.
Pneumologia (Bucharest, Romania) 0 61 (2): 84-7.
Nikibakhsh Ahmad-Ali, Houshmand Mohammad, Bagheri Morteza, Zadeh Hashem Mahmood, Rad Isa Ab
Familial Mediterranean fever in Germany: clinical presentation and amyloidosis risk.
Scandinavian journal of rheumatology 2013 42 (1): 52-8.
Ebrahimi-Fakhari D, Schönland S O, Hegenbart U, Lohse P, Beimler J, Wahlster L, Ho A D, Lorenz H-M, Blank
The genetics of Henoch-Schönlein purpura: a systematic review and meta-analysis.
Rheumatology international 2013 Jun 33 (6): 1387-95.
He Xuelian, Yu Chunhua, Zhao Peiwei, Ding Yan, Liang Xiaohui, Zhao Yulan, Yue Xin, Wu Yanxiang, Yin W
MEFV gene mutations in Egyptian children with Henoch-Schonlein purpura.
Pediatric rheumatology online journal 2014 12 41.
Salah Samia, Rizk Samia, Lotfy Hala M, El Houchi Salma, Marzouk Huda, Farag Yom
Vasculitis and long standing ankylosing spondylitis in a patient with familial Mediterranean fever.
Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2014 Oct 19 (10): 1009-11.
Taylan Ali, Yildiz Yasar, Sari Ismail, Ozkok Gul
Familial Mediterranean fever-associated diseases in children.
QJM : monthly journal of the Association of Physicians 2017 1 110 (5): 287-290.
Özçakar Z B, Çakar N, Uncu N, Çelikel B A, Yalçinkaya
Polyarteritis nodosa: lessons from 25 years of experience.
Clinical and experimental rheumatology 2018 11 37 Suppl 117 (2): 52-56.
Sönmez Hafize Emine, Arma?an Berkan, Ayan Gizem, Barut Kenan, Batu Ezgi Deniz, Erden Abdulsamet, U?urlu Serdal, Bilginer Yelda, Kasapçopur Özgur, Karada? Ömer, Bilgen Sule Apras, Özdo?an Huri, Ozen Se
Familial Mediterranean fever is associated with a wide spectrum of inflammatory disorders: results from a large cohort study.
Rheumatology international 2019 Aug .
Atas Nuh, Armagan Berkan, Bodakci Erdal, Satis Hasan, Sari Alper, Bilge Nazife Sule Yasar, Salman Reyhan Bilici, Yard?mc? Gozde Kubra, Babaoglu Hakan, Guler Aslihan Avanoglu, Karadeniz Hazan, Kilic Levent, Ozturk Mehmet Akif, Goker Berna, Haznedaroglu Seminur, Kalyoncu Umut, Kasifoglu Timucin, Tufan Abdurrahm
Kawasaki disease and familial mediterranean fever gene mutations, is there any link?
Open access rheumatology : research and reviews 2019 6 11 127-131.
Salehzadeh Farhad, Mirzarahimi Mehrdad, Hosseini Asl Saied, Nematdoust Haghi Roghay
Association of Vasculitis and Familial Mediterranean Fever.
Frontiers in immunology 2019 4 10 763.
Abbara Salam, Grateau Gilles, Ducharme-Bénard Stéphanie, Saadoun David, Georgin-Lavialle Soph
Optical coherence tomography-angiographic vascular densities in Familial Mediterranean Fever (FMF) Patients with M694V Mutations.
Ophthalmic genetics 2020 5 41 (3): 257-262.
Çavdarli Cemal, Çavdarli Büsranur, Topcu-Yilmaz Pinar, Polat Gültekin Bur
IgA Vasculitis in Japanese Patients Harboring MEFV Mutations: A Case Report and Review of the Literature.
Cureus 2023 3 15 (2): e34876.
Yokoyama Tadafumi, Sakumura Naoto, Inoue Natsumi, Matsuda Yusuke, Wada Tai
TOP